Gene: PRRT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112476
Gene Symbol: PRRT2
PRRT2 		0.120 GeneticVariation phenotype BEFREE PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state. 23398397 2013
Entrez Id: 112476
Gene Symbol: PRRT2
PRRT2 		0.120 GeneticVariation phenotype BEFREE We conclude that heterogeneous paroxysmal disorders are associated with PRRT2 mutations and include paroxysmal torticollis and hemiplegic migraine. 22845787 2012
Entrez Id: 112476
Gene Symbol: PRRT2
PRRT2 		0.120 Biomarker phenotype HPO